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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Carsten G. Bönnemann

Division of Neurology and Neuromuscular Program

The Children's Hospital of Philadelphia

Philadelphia

USA

[email]@*.chop.edu

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Affiliations

Division of Neurology and Neuromuscular Program, The Children's Hospital of Philadelphia, Philadelphia, USA. 2005
Division of Neurology, Children's Hospital of Philadelphia and University of Pennsylvania School of Medicine, 34th Strteet and Civic Center Boulevard, Philadelphia, USA. 2003 - 2004
Division of Genetics, Children's Hospital, Howard Hughes Medical Institute, USA. 2002

References

Limb-girdle muscular dystrophy in childhood. Bönnemann, C.G. Pediatr. Ann (2005) [Pubmed]
Myopathies resulting from mutations in sarcomeric proteins. Bönnemann, C.G., Laing, N.G. Curr. Opin. Neurol. (2004) [Pubmed]
Filamin C accumulation is a strong but nonspecific immunohistochemical marker of core formation in muscle. Bönnemann, C.G., Thompson, T.G., van der Ven, P.F., Goebel, H.H., Warlo, I., Vollmers, B., Reimann, J., Herms, J., Gautel, M., Takada, F., Beggs, A.H., Fürst, D.O., Kunkel, L.M., Hanefeld, F., Schröder, R. J. Neurol. Sci. (2003) [Pubmed]
Primary gamma-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile. Bönnemann, C.G., Wong, J., Jones, K.J., Lidov, H.G., Feener, C.A., Shapiro, F., Darras, B.T., Kunkel, L.M., North, K.N. Neuromuscul. Disord. (2002) [Pubmed]